S-silylmethyl-substituted ketene dithioacetals as synthetic equivalent of a novel 1,3-dipolar reagent, alkylidenethiocarbonyl ylide; synthesis and [3+2] cycloaddition reactions-Reference-Cited by-同舟云学术

S-silylmethyl-substituted ketene dithioacetals as synthetic equivalent of a novel 1,3-dipolar reagent, alkylidenethiocarbonyl ylide; synthesis and [3+2] cycloaddition reactions

Published:1994-05 Issue:21 Volume:35 Page:3555-3558
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Tominaga Yoshinori,Takada Satoshi,Kohra Shinya

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference15 articles.

1. Effect of a Silyl Group on the Regio- and Stereoselectivity in 1,3-Dipolar Cycloaddition

2. Generation of thiocarbonyl ylides with release of disiloxane from bis(trimethylsilylmethyl) sulfoxides

3. New synthesis of thiiranes by fluoride ion-promoted reaction of S-methyl-S′-trimethylsilylmethyl N-(p-toluenesulfonyl)dithioiminocarbonate and 2-(trimethylsilylmethylthio)thiazoline with aldehydes

4. Studies of organosilicon chemistry. 107. N-(silylmethyl)-substituted ketene N,S-acetals as a synthetic equivalent of a novel 1,3-dipolar reagent, alkylideneazomethine ylides: synthesis and [3 + 2] cycloadditions

5. Synthesis of indolizine derivatives and their related compounds using ketene dithioacetals.

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1. Recent developments of ketene dithioacetal chemistry;Chem. Soc. Rev.;2013

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5. One or More CC Bond(s) Formed by Substitution: Substitution of Carbon–Nitrogen, –Phosphorus, –Arsenic, –Antimony, –Boron, –Silicon, –Germanium, and –Metal Functions;Comprehensive Organic Functional Group Transformations II;2005